Apert syndrome - clinical case

Apert syndrome - acrocephalosyndactyly - is a rare autosomal dominant disorder representing 1:65 000 cases of living newborns. Characteristic malformations of the Apert syndrome are early craniostenosis, microviscerocranium and II-V finger syndactyly of hand and toes with proximal phalanx of the bil...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Romanian journal of morphology and embryology 2017, Vol.58 (1), p.277-280
Hauptverfasser:	Siminel, Mirela Anişoara, NeamŢu, Cristian Ovidiu, DiŢescu, Damian, ForŢofoiu, Mircea Cătălin, Comănescu, Alexandru Cristian, Novac, Marius Bogdan, NeamŢu, Simona Daniela, Gluhovschi, Adrian
Format:	Artikel
Sprache:	eng
Schlagworte:	Acrocephalosyndactylia - diagnostic imaging Acrocephalosyndactylia - pathology Female Humans Infant, Newborn Pregnancy Reticulocytosis Syndactyly - diagnostic imaging Syndactyly - pathology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!